ライフサイエンスコーパス: mucosal epithelial cell

1 type ranging from professional phagocytes to mucosal epithelial cells.

2 envelope glycoprotein (Env) interaction with mucosal epithelial cells.

3 coprotein expressed on the apical surface of mucosal epithelial cells.

4 nscytosed by the pIgA receptor (pIgR) across mucosal epithelial cells.

5 atively regulates DeltaNp73 transcription in mucosal epithelial cells.

6 coupled prostaglandin receptors expressed by mucosal epithelial cells.

7 ptor (pIgR) mediates transport of IgA across mucosal epithelial cells.

8 at are associated with increased invasion of mucosal epithelial cells.

9 fection may be facilitated by replication in mucosal epithelial cells.

10 extent by transcription of the PIGR gene in mucosal epithelial cells.

11 ing small molecule therapeutics and genes to mucosal epithelial cells.

12 and novel VCAM-1 expression by cutaneous and mucosal epithelial cells.

13 host defense, transporting antibodies across mucosal epithelial cells.

14 ponsible for specific interaction with human mucosal epithelial cells.

15 well defined how HIV-1 infects CD4-negative mucosal epithelial cells.

16 t had no effect on the growth rate of normal mucosal epithelial cells.

17 shed by specific binding to the cilia of the mucosal epithelial cells.

18 d cytotoxic effects marked by exfoliation of mucosal epithelial cells.

19 ytotoxin causes vacuolation of primary human mucosal epithelial cells.

20 r for HIV-1 envelope (Env) interactions with mucosal epithelial cells.

21 king their attachment to or penetration into mucosal epithelial cells, a common site of exposure to v

22 d by tropic binding to the apical surface of mucosal epithelial cells and cells lining gastric pits.

23 The cross talk between mucosal epithelial cells and DC, mediated by HIV-induced

24 istry data showed that IL-32 was detected in mucosal epithelial cells and inflammatory cells in the l

25 ciated epithelial chemokine), is secreted by mucosal epithelial cells and is found in saliva and in b

26 of IgA antibodies is to transport IgA across mucosal epithelial cells and not, as in the case of the

27 In contrast, mucosal epithelial cells and other mitotic cells respond

28 s act globally, IFN-lambdas primarily target mucosal epithelial cells and protect them against the fr

29 ral to gammaherpesvirus persistence, whereas mucosal epithelial cells are considered nonessential.

30 Epidermal and mucosal epithelial cells are integral to host defense.

31 liferation and differentiation of intestinal mucosal epithelial cells are not well understood.

32 Cutaneous and mucosal epithelial cells are primary targets of injury i

33 Mucosal epithelial cells are uniquely equipped to mainta

34 since C. albicans is closely associated with mucosal epithelial cells as a commensal, we sought to id

35 tor-1 (SDF-1) is constitutively expressed by mucosal epithelial cells at sites of HIV transmission an

36 er was unable to pass from the lumen between mucosal epithelial cells, because the presence of an int

37 e of genital herpes, infects oral or genital mucosal epithelial cells before infecting the peripheral

38 Squamous mucosal epithelial cells constitutively express calprote

39 Human gastric mucosal epithelial cells display class II MHC, the expre

40 The innate immune response of mucosal epithelial cells during pathogen invasion plays

41 eptors (GRP-R) are not normally expressed by mucosal epithelial cells except for those lining the gas

42 A antibodies against RTA and RTB can protect mucosal epithelial cells from ricin intoxication.

43 Cutaneous and mucosal epithelial cells function as both a physical bar

44 iRNAs thus have an indirect effect on lining mucosal epithelial cell growth/differentiation.

45 IL-22 plays an important role in mucosal epithelial cell homeostasis.

46 Minimal to mild colitis with mucosal epithelial cell hyperplasia of the colon was mos

47 itis was characterized by moderate to marked mucosal epithelial cell hyperplasia with mild monocytic

48 to the polymeric immunoglobulin receptor on mucosal epithelial cells, IgA antibodies can bind to rec

49 n Bak was reduced compared to that of normal mucosal epithelial cells in 27 of 30 (90%) carcinomas an

50 mmensal organisms have a role in stimulating mucosal epithelial cells in maintaining the barrier that

51 onstrate that B7-1 and B7-2 are expressed on mucosal epithelial cells in situ.

52 des new findings regarding the role of local mucosal epithelial cells in the initiation of ocular all

53 Mucosal epithelial cells in the respiratory tract act as

54 membrane of chlamydiae that are involved in mucosal epithelial cell infection must clearly be identi

55 SIgA is transported across glandular and mucosal epithelial cells into external secretions by the

56 suggest that HIV-mediated TSLP production by mucosal epithelial cells is a critical trigger for DC-me

57 bacterium, efficient colonization of genital mucosal epithelial cells is crucial to the infectious pr

58 enocytes and on the apical surfaces of human mucosal epithelial cell monolayers.

59 i.e., FGFR4 and betaKlotho) are expressed in mucosal epithelial cells of the gallbladder and small in

60 le of TLR signaling in immune defense of the mucosal epithelial cells of the lower female genital tra

61 Transplantation of cultured oral mucosal epithelial cells (OMECs) is a promising treatmen

62 Since mucosal epithelial cells produce a variety of cytokines

63 linaclotide: it activates GC-C expressed on mucosal epithelial cells, resulting in the production an

64 OSR) using tissue-engineered cultivated oral mucosal epithelial cell sheets (COMECS) is a promising n

65 found in intestinal capillaries and between mucosal epithelial cells, suggesting that the microvascu

66 Mucosal epithelial cell surface galactosylceramide (Galc

67 cationic antimicrobial peptides, secreted by mucosal epithelial cells that regulate adaptive immune f

68 to the intensity observed in adjacent normal mucosal epithelial cells, the intensity of Bcl-X immunos

69 Mucosal epithelial cells thus express a plasmalemmal 5-H

70 to keratinocytes and heterotypic adhesion of mucosal epithelial cells to E-cadherin-negative intestin

71 tely understood, it is known that CT induces mucosal epithelial cells to produce the proinflammatory

72 We report that HIV induces human genital mucosal epithelial cells to produce thymic stromal lymph

73 mucin-galectin interaction in four different mucosal epithelial cell types using competitive carbohyd

74 e body by transporting them directly through mucosal epithelial cells, using the same mechanism that

75 osal signaling is inactivated by uptake into mucosal epithelial cells, which are mediated by an integ